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A Young Family Navigating Spinal Muscular Atrophy (SMA)
Clip: Season 1 | 4m 30s
| Video has closed captioning.
This excerpt is the story of a young family with two children who have spinal muscular atrophy (SMA). SMA is a rare genetic neuromuscular disease that affects the part of the nervous system that controls voluntary muscle movement. It is a deteriorating disease — and children with this form of SMA may survive to two years of age or older.
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Funding for KEN BURNS PRESENTS THE GENE: AN INTIMATE HISTORY has been provided by Genentech, 23andMe, Cancer Treatment Centers of America, Alfred P. Sloan Foundation, Gray Foundation, American Society of …
Funding for KEN BURNS PRESENTS THE GENE: AN INTIMATE HISTORY has been provided by Genentech, 23andMe, Cancer Treatment Centers of America, Alfred P. Sloan Foundation, Gray Foundation, American Society of Clinical Oncology (ASCO) & Conquer Cancer Foundation, Judy and Peter Blum Kovler Foundation, Craig and Susan McCaw Foundation, and the Corporation for Public Broadcasting. The Outreach and Education Partner is National Institutes of Health, National Human Genome Research Institute. Outreach support is provided by Foundation Medicine.
What the heck is a gene, anyway? This animated series won’t get you a PhD, but it does clear up a few mysteries about how genes work and what they might look like in the future. (Microscope not required.)
